K. Fujiki

发表

Transferrin-polyethylenimine conjugate, FuGENE6 and TransIT-LT as nonviral vectors for gene transfer to the corneal endothelium.

A. Murakami, T. H. Nguyen, K. Fujiki, 2002, Japanese journal of ophthalmology.

Results and transition of treatment of keratoconus over 41 years in Juntendo university hospital

A. Murakami, K. Fujiki, A. Kanai, 2003 .

Analysis of phosducin as a candidate gene for retinopathies.

S. Jacobson, K. Fujiki, M. Hayakawa, 1996, Ophthalmic genetics.

In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy

A. Murakami, K. Fujiki, Ai Yanagawa, 2018, Japanese Journal of Ophthalmology.

Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy.

K. Fujiki, A. Kanai, Y. Hotta, 2000, American journal of ophthalmology.

Distribution of goblet cells and MUC5AC mRNA in the canine nictitating membrane.

A. Murakami, K. Fujiki, H. Toshida, 2010, Experimental eye research.

High resolution G-banding analysis in aniridia.

K. Fujiki, A. Nakajima, Y. Hotta, 1987, Ophthalmic paediatrics and genetics.

for retinopathies Analysis of phosducin as a candidate gene

S. Jacobson, K. Fujiki, M. Hayakawa, 1996 .

Multicenter genetic study of retinitis pigmentosa in Japan: I. Genetic heterogeneity in typical retinitis pigmentosa.

M. Matsumura, M. Tamai, K. Wakabayashi, 1997, Japanese journal of ophthalmology.

Studies on the mechanism of early onset macular degeneration in cynomolgus monkeys. II. Suppression of metallothionein synthesis in the retina in oxidative stress.

K. Fujiki, Y. Yoshikawa, N. Shindo, 1996, Experimental eye research.

A novel mutation (967−970+2)delAAAGGT in the choroideremia gene found in a Japanese family and related clinical findings

A. Murakami, K. Fujiki, T. Fujimaki, 2008, Japanese Journal of Ophthalmology.

Visual impairment and REP-1 gene mutations in Japanese choroideremia patients.

E. Kominami, K. Fujiki, A. Kanai, 1999, Ophthalmic genetics.

[Candidate gene approach].

Y. Hotta, K. Fujiki, 1996, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

Analysis of COL8A2 Gene Mutation in Japanese Patients with Fuchs’ Endothelial Dystrophy and Posterior Polymorphous Dystrophy

A. Murakami, K. Fujiki, A. Kanai, 2004, Japanese Journal of Ophthalmology.

A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy

A. Murakami, K. Fujiki, A. Kanai, 2008, Japanese Journal of Ophthalmology.

Birth order and parental age in microphthalmos and other ocular diseases.

K. Fujiki, A. Nakajima, N. Yasuda, 1979, American journal of ophthalmology.

Incidence of congenital malformations in Tokyo Metropolitan Hospitals, 1979–1993

K. Fujiki, Kyoko Kato, 1996, Brain and Development.

Tear chymase in vernal keratoconjunctivitis

A. Murakami, S. Takai, M. Miyazaki, 2004, Current eye research.

OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy

A. Murakami, A. Miyazaki, K. Fujiki, 2011, Japanese Journal of Ophthalmology.

OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484.

A. Murakami, K. Fujiki, A. Kanai, 2003, Japanese journal of ophthalmology.

Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I

A. Murakami, X. Tian, K. Fujiki, 2005, Japanese Journal of Ophthalmology.

A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy.

A. Murakami, K. Fujiki, A. Kanai, 2003, Japanese journal of ophthalmology.

Corneal dystrophies in Japan

K. Fujiki, A. Kanai, K. Nakayasu, 2001, Journal of Human Genetics.

Clinical findings in a choroideremia patient who underwent vitrectomy for retinal detachment associated with macular hole

K. Tsubota, A. Murakami, Y. Ozawa, 2011, Japanese Journal of Ophthalmology.

Multicenter genetic study of retinitis pigmentosa in Japan: II. Prevalence of autosomal recessive retinitis pigmentosa.

M. Matsumura, M. Tamai, K. Wakabayashi, 1997, Japanese journal of ophthalmology.

Studies on the mechanism of early onset macular degeneration in cynomolgus (Macaca fascicularis) monkeys. I. Abnormal concentrations of two proteins in the retina.

K. Murayama, Y. Yoshikawa, K. Fujiki, 1996, Experimental eye research.

Expression and Distribution of Junctional Adhesion Molecule-1 in the Human Cornea

A. Murakami, K. Fujiki, N. Ebihara, 2007, Japanese Journal of Ophthalmology.

In vivo laser confocal microscopy findings and mutational analysis for Schnyder's crystalline corneal dystrophy.

A. Murakami, K. Fujiki, K. Sugiyama, 2009, Ophthalmology.

Screening of Candidate Genes on Japanese Retinal Dystrophies

H. Kawano, A. Murakami, M. Tamai, 1997 .

Multiplex polymerase chain reaction for detection of herpes simplex virus type 1, type 2, cytomegalovirus, and varicella-zoster virus in ocular viral infections.

A. Murakami, K. Fujiki, A. Kanai, 2003, Japanese Journal of Ophthalmology.

In vivo laser confocal microscopic findings of corneal stromal dystrophies.

A. Murakami, K. Fujiki, K. Sugiyama, 2007, Archives of ophthalmology.

[Estimation of patient visit rate and incidence of keratoconus in the 23 wards of Tokyo].

K. Fujiki, K. Nakayasu, R. Ota, 2002, Nippon Ganka Gakkai zasshi.

Homozygotic Patient with βig‐h3 Gene Mutation in Granular Dystrophy

K. Fujiki, A. Kanai, Y. Hotta, 1998, Cornea.

Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.

A. Murakami, K. Fujiki, A. Kanai, 2003, Investigative ophthalmology & visual science.

Late-onset Form of Lattice Corneal Dystrophy Caused by Leu527Arg Mutation of the TGFBI Gene

K. Fujiki, A. Kanai, Y. Hotta, 2001, Cornea.

Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene

K. Fujiki, A. Kanai, Y. Hotta, 2000 .

Mutation Analysis of CHST6 Gene in Chinese Patients With Macular Corneal Dystrophy

A. Murakami, X. Tian, K. Fujiki, 2010, Cornea.

A new L527R mutation of the βIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities

Tatsuo Yamaguchi, K. Fujiki, A. Kanai, 1998, Human Genetics.

[Prevalence of keratoconus patients in Japan].

K. Fujiki, A. Kanai, U. Tanabe, 1985, Nippon Ganka Gakkai zasshi.

Arg124Cys mutation of the betaig-h3 bene in a Japanese family with lattice corneal dystrophy type I.

K. Fujiki, A. Kanai, Y. Hotta, 1999, Japanese journal of ophthalmology.

Six Different Mutations of TGFBI (&bgr;ig-h3, Keratoepithelin) Gene Found in Japanese Corneal Dystrophies

K. Fujiki, A. Kanai, T. Kato, 2000, Cornea.

Leu518Pro mutation of the βig-h3 gene causes lattice corneal dystrophy type I

Tatsuo Yamaguchi, K. Fujiki, A. Kanai, 1999 .

Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type I.

K. Fujiki, A. Kanai, Y. Hotta, 1999, American journal of ophthalmology.

Identification of Novel Mutations of the CHST6 Gene in Vietnamese Families Affected With Macular Corneal Dystrophy in Two Generations

Y. Hiratsuka, A. Murakami, K. Fujiki, 2003, Cornea.

[Gene transfer into corneal endothelial cells by Helios gene gun].

K. Fujiki, A. Kanai, N. Ebihara, 2003, Nippon Ganka Gakkai zasshi.

Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.

Y. Hiratsuka, A. Murakami, K. Fujiki, 2003, Investigative ophthalmology & visual science.

Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification.

K. Fujiki, A. Kanai, M. Hayakawa, 1989, American journal of ophthalmology.

Plus/minus screening of rabbit corneal endothelial cDNA library.

K. Fujiki, A. Kanai, Y. Hotta, 1997, Japanese journal of ophthalmology.

Long-term Follow-up of Two Sisters with Leber's Hereditary Optic Neuropathy

A. Murakami, K. Fujiki, Y. Hotta, 2005, Japanese Journal of Ophthalmology.

A hemizygous A to CC base change of theCHM gene causing choroideremia associated with pinealoma

K. Fujiki, A. Kanai, M. Hayakawa, 1997, Graefe's Archive for Clinical and Experimental Ophthalmology.

REP-1 gene mutations in Japanese patients with choroideremia

A. Murakami, K. Fujiki, A. Kanai, 1999, Graefe's Archive for Clinical and Experimental Ophthalmology.

Mutation Spectrum in the Rep-1 Gene of Japanese Choroideremia Patients

A. Murakami, K. Fujiki, A. Kanai, 1999 .

Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene

K. Fujiki, A. Kanai, M. Hayakawa, 1998, Human Genetics.

Japanese juvenile retinoschisis is caused by mutations of the

K. Fujiki, A. Kanai, M. Hayakawa, 1998 .

[A case of juvenile retinoschisis diagnosed by analysis of the XLRS 1 gene].

K. Fujiki, A. Kanai, Y. Hotta, 2000, Nippon Ganka Gakkai zasshi.

H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people

A. Murakami, K. Fujiki, A. Kanai, 2003, The British journal of ophthalmology.

Genetic analysis of microphthalmos

K. Kabasawa, K. Fujiki, A. Nakajima, 1982 .

Visual Function in Retinitis pigmentosa Related to a Codon 15 Rhodopsin Gene Mutation

A. Murakami, K. Fujiki, A. Kanai, 1998, Ophthalmic Research.

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)

R. Kawaguchi, M. Tamai, K. Fujiki, 1992, Japanese Journal of Human Genetics.

A Family with X-Linked Cone Dystrophy Showing a Tapetal-Like Reflex

I. Kondo, K. Fujiki, A. Kanai, 1997 .

Molecular cloning of ELOVL4 gene from cynomolgus monkey (Macaca fascicularis).

F. Ono, K. Fujiki, A. Kanai, 2002, Experimental animals.

Molecular Cloning of ELOVL 4 Gene from Cynomolgus Monkey ( Macaca fascicularis )

F. Ono, K. Fujiki, A. Kanai, 2003 .

Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.

K. Fujiki, A. Kanai, M. Hayakawa, 1995, Japanese journal of ophthalmology.

Mutation Analysis of the TGFBI Gene in Vietnamese with Granular and Avellino Corneal Dystrophy

Y. Hiratsuka, A. Murakami, K. Fujiki, 2003, Japanese Journal of Ophthalmology.

A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation

A. Murakami, K. Fujiki, T. Fujimaki, 2007, Japanese Journal of Ophthalmology.

Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778

K. Fujiki, A. Kanai, Y. Hotta, 1998, Journal of Human Genetics.

Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.

K. Fujiki, A. Kanai, Y. Hotta, 1999, Ophthalmic genetics.

A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathy

K. Fujiki, A. Kanai, K. Yanashima, 1991, Japanese Journal of Human Genetics.

[Polygenic analysis of keratoconus].

K. Fujiki, A. Kanai, M. Itoi, 1985, Nippon Ganka Gakkai zasshi.

[Case of late onset and isolated lattice corneal dystrophy with Asn544Ser (N544S) mutation of transforming growth factor beta-induced (TGFBI, BIGH3) gene].

A. Murakami, K. Fujiki, A. Kanai, 2004, Nippon Ganka Gakkai zasshi.

High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.

M. Inoue, M. Yamada, K. Fujiki, 1992, Japanese journal of ophthalmology.

[A trial of molecular diagnosis in Leber's optic neuropathy].

K. Fujiki, A. Kanai, K. Yanashima, 1991, Nippon Ganka Gakkai zasshi.

Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.

H. Kawano, A. Murakami, K. Fujiki, 2002, American journal of ophthalmology.

Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient.

K. Fujiki, A. Kanai, K. Yanashima, 1993, American journal of ophthalmology.

[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa].

M. Tamai, K. Fujiki, A. Kanai, 1992, Nippon Ganka Gakkai zasshi.

Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.

M. Tamai, K. Fujiki, A. Kanai, 1992, Japanese journal of ophthalmology.

Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa

A. Murakami, K. Fujiki, A. Kanai, 1995, Japanese Journal of Human Genetics.

Analysis of peripherin/RDS gene for Japanese retinal dystrophies.

K. Fujiki, A. Kanai, M. Hayakawa, 1998, Japanese journal of ophthalmology.

Frequencies of polymorphisms in the rhodopsin gene of Japanese retinitis pigmentosa and normal individuals

H. Kawano, K. Fujiki, A. Kanai, 1995, Japanese Journal of Human Genetics.

Mutations in the Membrane Component, Chromosome 1, Surface Marker 1 (M1S1) Gene in Gelatinous Drop-like Corneal Dystrophy

A. Murakami, K. Fujiki, A. Kanai, 2004, Japanese Journal of Ophthalmology.

Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy.

A. Murakami, X. Tian, K. Fujiki, 2004, American journal of ophthalmology.

A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy.

A. Murakami, K. Fujiki, A. Kanai, 2003, American journal of ophthalmology.

Corneal amyloidosis caused by Leu 518 Pro mutation of â igh 3 gene

K. Fujiki, A. Kanai, Y. Hotta, 2000 .

Effects of parental age and birth order in motor neuron disease

K. Fujiki, K. Kondo, 1984, Japanese Journal of Human Genetics.

Recent aspect of optic neuropathy

K. Fujiki, Y. Hotta, 1999 .

A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis

A. Murakami, K. Fujiki, Ai Yanagawa, 2014, Japanese Journal of Ophthalmology.

A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosa.

K. Fujiki, M. Hayakawa, R. Weleber, 1995, Genomics.

Mutations in the Norrie disease gene: a new mutation in a Japanese family.

K. Fujiki, M. Hayakawa, N. Ohba, 1995, The British journal of ophthalmology.

An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

K. Fujiki, A. Kanai, K. Yanashima, 1993, The British journal of ophthalmology.

A Case Report of Oculofaciocardiodental Syndrome With Novel BCOR Gene Mutation

H. Kawano, A. Murakami, K. Fujiki, 2008 .

Multiple births and congenital anomalies in Tokyo Metropolitan Hospitals, 1979-1990.

K. Fujiki, K. Kato, 1992, Acta geneticae medicae et gemellologiae.

Genetic epidemiology of duchenne muscular dystrophy in Japan: Classical segregation analysis

N. Morton, I. Borecki, M. Kanamori, 1987, Genetic epidemiology.

Familial cases of Norrie disease detected by copy number analysis

K. Fujiki, Ai Yanagawa, Eisuke Arai, 2014, Japanese Journal of Ophthalmology.

A research of consanguinity in Japanese young couples

K. Fujiki, A. Nakajima, Y. Hosoda, 1983, Japanese Journal of Human Genetics.

Genetic Mechanism in Man

K. Fujiki, 1986 .